Canonical Allele Identifier: CA403331277

Gene: TBXA2R

Linked Data

• dbSNP Id: rs1460450992
• gnomAD v2: 19-3595911-C-T
• gnomAD v4: 19-3595913-C-T
• MyVariant Identifiers: chr19:g.3595911C>T (hg19) ; chr19:g.3595913C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.3595913C>T , CM000681.2:g.3595913C>T	GRCh38
NC_000019.9:g.3595911C>T , CM000681.1:g.3595911C>T	GRCh37
NC_000019.8:g.3546911C>T	NCBI36
NG_013363.1:g.15921G>A , LRG_578:g.15921G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375190.10:c.807G>A MANE Select	ENSP00000364336.4:p.Val269=
ENST00000375190.8:c.807G>A	ENSP00000364336.3:p.Val269=
ENST00000411851.3:c.807G>A	ENSP00000393333.2:p.Val269=
ENST00000589966.1:c.418G>A	ENSP00000468145.1:p.Ala140Thr
NM_001060.5:c.807G>A , LRG_578t1:c.807G>A	NP_001051.1:p.Val269=
NM_201636.2:c.807G>A	NP_963998.2:p.Val269=
XM_011528214.1:c.807G>A	XP_011526516.1:p.Val269=
XM_011528214.2:c.807G>A	XP_011526516.1:p.Val269=
NM_001060.6:c.807G>A MANE Select	NP_001051.1:p.Val269=
NM_201636.3:c.807G>A	NP_963998.2:p.Val269=